| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| FAM169A | Colorectal Cancer | p004_CRC_A01 | Chr5:74134927:G>A | Branch mutation |
| FAM169A | Esophageal Squamous Cell Carcinoma | p139_EC0949 | p.S12R | Private mutation |
| FAM169A | Esophageal Squamous Cell Carcinoma | p139_EC0949 | p.S12N | Private mutation |
| FAM169A | Gastric Adenocarcinoma | p011_MSI-H1 | p.P490T | Private mutation |
| FAM169A | Gastric Carcinoma | p106_GC07 | p.K146T | Private mutation |
| FAM169A | Medulloblastoma | p072_MB6 | Chr5:74226440:A>C | Branch mutation |
| FAM169A | Medulloblastoma | p072_MB6 | Chr5:74226441:A>G | Branch mutation |
| FAM169A | Clear Cell Renal Cell Carcinoma | p019_RK26 | Chr5:74078809:p.V>F | Branch mutation |
| FAM169A | Renal Cell Carcinoma | p073_RCC7 | Chr5:74078809:C>A | Branch mutation |